
PubMed:9134435
Annnotations
Glycan-Motif
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 24-33 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T2 | 123-132 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T3 | 286-295 | https://glytoucan.org/Structures/Glycans/G00058MO | denotes | i antigen |
T4 | 326-335 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T5 | 339-359 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamines |
T6 | 507-526 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamine |
T7 | 1427-1436 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T8 | 1900-1909 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T9 | 2149-2158 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
GlyCosmos6-Glycan-Motif-Image
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 24-33 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
T5 | 123-132 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
T9 | 286-295 | Glycan_Motif | denotes | i antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00058MO |
T10 | 326-335 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
T14 | 339-359 | Glycan_Motif | denotes | N-acetyllactosamines | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00055MO |
T15 | 507-526 | Glycan_Motif | denotes | N-acetyllactosamine | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00055MO |
T16 | 1427-1436 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
T20 | 1900-1909 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
T24 | 2149-2158 | Glycan_Motif | denotes | I antigen | https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G56045WU|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G46055MA|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G45207BM|https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G26929DQ |
Glycosmos6-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 24-33 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
T2 | 123-132 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
T3 | 286-295 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | i antigen |
T4 | 326-335 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
T5 | 1427-1436 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
T6 | 1900-1909 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
T7 | 2149-2158 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
TextSentencer_T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
TextSentencer_T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
TextSentencer_T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
TextSentencer_T5 | 447-655 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. |
TextSentencer_T6 | 656-664 | Sentence | denotes | Embryol. |
TextSentencer_T7 | 665-669 | Sentence | denotes | Exp. |
TextSentencer_T8 | 670-694 | Sentence | denotes | Morphol., 87, 115-128.). |
TextSentencer_T9 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
TextSentencer_T10 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
TextSentencer_T11 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
TextSentencer_T12 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
TextSentencer_T13 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
TextSentencer_T14 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
TextSentencer_T15 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
TextSentencer_T16 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
TextSentencer_T17 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
TextSentencer_T18 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
TextSentencer_T19 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
TextSentencer_T20 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
T5 | 447-694 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. Embryol. Exp. Morphol., 87, 115-128.). |
T6 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
T7 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
T8 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
T9 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
T10 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
T11 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
T12 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
T13 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
T14 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
T15 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
T16 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
T17 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
T5 | 447-655 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. |
T6 | 656-664 | Sentence | denotes | Embryol. |
T7 | 665-669 | Sentence | denotes | Exp. |
T8 | 670-694 | Sentence | denotes | Morphol., 87, 115-128.). |
T9 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
T10 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
T11 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
T12 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
T13 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
T14 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
T15 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
T16 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
T17 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
T18 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
T19 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
T20 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
GlyCosmos6-Glycan-Motif-Structure
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 24-33 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T2 | 123-132 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T3 | 286-295 | https://glytoucan.org/Structures/Glycans/G00058MO | denotes | i antigen |
T4 | 326-335 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T5 | 339-359 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamines |
T6 | 507-526 | https://glytoucan.org/Structures/Glycans/G00055MO | denotes | N-acetyllactosamine |
T7 | 1427-1436 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T8 | 1900-1909 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
T9 | 2149-2158 | https://glytoucan.org/Structures/Glycans/G26929DQ | denotes | I antigen |
GlycoBiology-FMA
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
_T1 | 94-101 | FMAID:256050 | denotes | tissues |
_T2 | 258-270 | FMAID:82737 | denotes | carbohydrate |
_T3 | 258-270 | FMAID:197276 | denotes | carbohydrate |
_T4 | 302-310 | FMAID:226028 | denotes | branched |
_T5 | 302-310 | FMAID:226027 | denotes | branched |
_T6 | 339-359 | FMAID:196780 | denotes | N-acetyllactosamines |
_T7 | 339-359 | FMAID:82786 | denotes | N-acetyllactosamines |
_T8 | 433-445 | FMAID:167137 | denotes | erythrocytes |
_T9 | 433-445 | FMAID:62845 | denotes | erythrocytes |
_T10 | 507-526 | FMAID:82786 | denotes | N-acetyllactosamine |
_T11 | 507-526 | FMAID:196780 | denotes | N-acetyllactosamine |
_T12 | 1047-1054 | FMAID:67257 | denotes | protein |
_T13 | 1047-1054 | FMAID:165447 | denotes | protein |
_T14 | 1114-1124 | FMAID:167180 | denotes | antibodies |
_T15 | 1145-1155 | FMAID:82740 | denotes | Nucleotide |
_T16 | 1145-1155 | FMAID:196729 | denotes | Nucleotide |
_T17 | 1254-1264 | FMAID:167180 | denotes | antibodies |
_T18 | 1288-1295 | FMAID:165447 | denotes | protein |
_T19 | 1288-1295 | FMAID:67257 | denotes | protein |
_T20 | 1392-1399 | FMAID:256050 | denotes | tissues |
_T21 | 1537-1543 | FMAID:256050 | denotes | tissue |
_T22 | 1678-1685 | FMAID:165447 | denotes | protein |
_T23 | 1678-1685 | FMAID:67257 | denotes | protein |
_T24 | 1745-1752 | FMAID:67257 | denotes | protein |
_T25 | 1745-1752 | FMAID:165447 | denotes | protein |
_T26 | 1753-1761 | FMAID:167180 | denotes | antibody |
_T27 | 1781-1793 | FMAID:82737 | denotes | carbohydrate |
_T28 | 1781-1793 | FMAID:197276 | denotes | carbohydrate |
_T29 | 1917-1936 | FMAID:165528 | denotes | in epithelial cells |
_T30 | 1917-1936 | FMAID:67559 | denotes | in epithelial cells |
_T31 | 1920-1936 | FMAID:66768 | denotes | epithelial cells |
_T32 | 1920-1936 | FMAID:67799 | denotes | epithelial cells |
_T33 | 1920-1936 | FMAID:197786 | denotes | epithelial cells |
_T34 | 1920-1936 | FMAID:83514 | denotes | epithelial cells |
_T35 | 1920-1936 | FMAID:164922 | denotes | epithelial cells |
_T36 | 1920-1936 | FMAID:69075 | denotes | epithelial cells |
_T37 | 1920-1936 | FMAID:169652 | denotes | epithelial cells |
_T38 | 1920-1936 | FMAID:69074 | denotes | epithelial cells |
_T39 | 1920-1936 | FMAID:165731 | denotes | epithelial cells |
_T40 | 1920-1936 | FMAID:169653 | denotes | epithelial cells |
_T41 | 1931-1936 | FMAID:68646 | denotes | cells |
_T42 | 1931-1936 | FMAID:169002 | denotes | cells |
_T43 | 1950-1955 | FMAID:68646 | denotes | cells |
_T44 | 1950-1955 | FMAID:169002 | denotes | cells |
_T45 | 2001-2006 | FMAID:169002 | denotes | cells |
_T46 | 2001-2006 | FMAID:68646 | denotes | cells |
_T47 | 2030-2037 | FMAID:50594 | denotes | surface |
_T48 | 2030-2037 | FMAID:146300 | denotes | surface |
_T49 | 2030-2048 | FMAID:67640 | denotes | surface of tissues |
_T50 | 2030-2048 | FMAID:165563 | denotes | surface of tissues |
_T51 | 2030-2048 | FMAID:118150 | denotes | surface of tissues |
_T52 | 2041-2048 | FMAID:256050 | denotes | tissues |
_T53 | 2215-2224 | FMAID:67498 | denotes | organisms |
_T54 | 2215-2224 | FMAID:166081 | denotes | organisms |
uniprot-human
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 51-82 | http://www.uniprot.org/uniprot/Q06430 | denotes | N-acetylglucosaminyltransferase |
T2 | 170-201 | http://www.uniprot.org/uniprot/Q06430 | denotes | N-acetylglucosaminyltransferase |
T3 | 51-82 | http://www.uniprot.org/uniprot/Q8N0V5 | denotes | N-acetylglucosaminyltransferase |
T4 | 170-201 | http://www.uniprot.org/uniprot/Q8N0V5 | denotes | N-acetylglucosaminyltransferase |
T5 | 51-82 | http://www.uniprot.org/uniprot/Q8NFS9 | denotes | N-acetylglucosaminyltransferase |
T6 | 170-201 | http://www.uniprot.org/uniprot/Q8NFS9 | denotes | N-acetylglucosaminyltransferase |
uniprot-mouse
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 51-82 | http://www.uniprot.org/uniprot/P97402 | denotes | N-acetylglucosaminyltransferase |
T2 | 170-201 | http://www.uniprot.org/uniprot/P97402 | denotes | N-acetylglucosaminyltransferase |
T3 | 665-668 | http://www.uniprot.org/uniprot/Q9JKP5 | denotes | Exp |
GlycoBiology-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 42-46 | http://purl.bioontology.org/ontology/NCBITAXON/3554 | denotes | beta |
T2 | 42-46 | http://purl.bioontology.org/ontology/NCBITAXON/158455 | denotes | beta |
T3 | 94-101 | http://purl.bioontology.org/ontology/STY/T024 | denotes | tissues |
T4 | 161-165 | http://purl.bioontology.org/ontology/NCBITAXON/3554 | denotes | beta |
T5 | 161-165 | http://purl.bioontology.org/ontology/NCBITAXON/158455 | denotes | beta |
T6 | 1145-1164 | http://purl.bioontology.org/ontology/STY/T086 | denotes | Nucleotide sequence |
T7 | 1392-1399 | http://purl.bioontology.org/ontology/STY/T024 | denotes | tissues |
T8 | 1537-1543 | http://purl.bioontology.org/ontology/STY/T024 | denotes | tissue |
T9 | 1931-1936 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T10 | 1950-1955 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T11 | 2001-2006 | http://purl.bioontology.org/ontology/STY/T025 | denotes | cells |
T12 | 2041-2048 | http://purl.bioontology.org/ontology/STY/T024 | denotes | tissues |
GO-BP
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 414-423 | http://purl.obolibrary.org/obo/GO_0065007 | denotes | regulated |
T2 | 722-732 | http://purl.obolibrary.org/obo/GO_0065007 | denotes | regulation |
T3 | 456-477 | http://purl.obolibrary.org/obo/GO_0009790 | denotes | embryonic development |
T4 | 466-477 | http://purl.obolibrary.org/obo/GO_0032502 | denotes | development |
T5 | 765-776 | http://purl.obolibrary.org/obo/GO_0032502 | denotes | development |
T6 | 2190-2201 | http://purl.obolibrary.org/obo/GO_0032502 | denotes | development |
T7 | 787-798 | http://purl.obolibrary.org/obo/GO_0006351 | denotes | transcripts |
T8 | 1475-1488 | http://purl.obolibrary.org/obo/GO_0006351 | denotes | transcription |
T9 | 1339-1343 | http://purl.obolibrary.org/obo/GO_0004617 | denotes | sera |
T10 | 1842-1846 | http://purl.obolibrary.org/obo/GO_0004617 | denotes | sera |
T11 | 1467-1488 | http://purl.obolibrary.org/obo/GO_0001171 | denotes | reverse-transcription |
GO-MF
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1114-1124 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | antibodies |
T2 | 1254-1264 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | antibodies |
T3 | 1753-1761 | http://purl.obolibrary.org/obo/GO_0003823 | denotes | antibody |
GO-CC
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 221-226 | http://purl.obolibrary.org/obo/GO_0005794 | denotes | Golgi |
T2 | 1931-1936 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T3 | 1950-1955 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
T4 | 2001-2006 | http://purl.obolibrary.org/obo/GO_0005623 | denotes | cells |
UBERON-AE
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 94-101 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissues |
T2 | 1392-1399 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissues |
T3 | 1537-1543 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissue |
T4 | 2209-2224 | http://purl.obolibrary.org/obo/UBERON_0007023 | denotes | adult organisms |
T5 | 2215-2224 | http://purl.obolibrary.org/obo/UBERON_0000062 | denotes | organisms |
GlycoBiology-Epitope
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-GlycoEpitope-B_T1 | 24-33 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T2 | 123-132 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T3 | 286-295 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | i antigen |
PD-GlycoEpitope-B_T4 | 326-335 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T5 | 1427-1436 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T6 | 1900-1909 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T7 | 2149-2158 | http://www.glycoepitope.jp/epitopes/EP0138 | denotes | I antigen |
PD-GlycoEpitope-B_T8 | 24-33 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
PD-GlycoEpitope-B_T9 | 123-132 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
PD-GlycoEpitope-B_T10 | 286-295 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | i antigen |
PD-GlycoEpitope-B_T11 | 326-335 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
PD-GlycoEpitope-B_T12 | 1427-1436 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
PD-GlycoEpitope-B_T13 | 1900-1909 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
PD-GlycoEpitope-B_T14 | 2149-2158 | http://www.glycoepitope.jp/epitopes/EP0139 | denotes | I antigen |
performance-test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
PD-UBERON-AE-B_T1 | 2215-2224 | http://purl.obolibrary.org/obo/UBERON_0000062 | denotes | organisms |
PD-UBERON-AE-B_T2 | 94-101 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissues |
PD-UBERON-AE-B_T3 | 1392-1399 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissues |
PD-UBERON-AE-B_T4 | 1537-1543 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissue |
PD-UBERON-AE-B_T5 | 2041-2048 | http://purl.obolibrary.org/obo/UBERON_0000479 | denotes | tissues |
PD-UBERON-AE-B_T6 | 2209-2224 | http://purl.obolibrary.org/obo/UBERON_0007023 | denotes | adult organisms |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 896-911 | Disease | denotes | teratocarcinoma | http://purl.obolibrary.org/obo/MONDO_0002599 |
Glycan-GlyCosmos
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 24-33 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T2 | 123-132 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T3 | 286-295 | Glycan | denotes | i antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G00058MO |
T4 | 326-335 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T5 | 1427-1436 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T6 | 1900-1909 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T7 | 2149-2158 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
GlyCosmos-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 24-33 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T2 | 123-132 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T3 | 286-295 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | i antigen | http://www.glycoepitope.jp/epitopes/EP0139 |
T4 | 326-335 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T5 | 1427-1436 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T6 | 1900-1909 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T7 | 2149-2158 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
GlyCosmos15-NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 111-115 | OrganismTaxon | denotes | mice | 10088 |
T2 | 427-432 | OrganismTaxon | denotes | human | 9606 |
T3 | 450-455 | OrganismTaxon | denotes | mouse | 10088|10090 |
T5 | 759-764 | OrganismTaxon | denotes | mouse | 10088|10090 |
T7 | 987-992 | OrganismTaxon | denotes | human | 9606 |
T8 | 1321-1326 | OrganismTaxon | denotes | human | 9606 |
T9 | 1386-1391 | OrganismTaxon | denotes | mouse | 10088|10090 |
T11 | 1824-1829 | OrganismTaxon | denotes | human | 9606 |
GlyCosmos15-CL
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 433-445 | Cell | denotes | erythrocytes | http://purl.obolibrary.org/obo/CL:0000232 |
T2 | 502-506 | Cell | denotes | poly | http://purl.obolibrary.org/obo/CL:0000096|http://purl.obolibrary.org/obo/CL:0000775 |
T4 | 1920-1936 | Cell | denotes | epithelial cells | http://purl.obolibrary.org/obo/CL:0000066 |
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TextSentencer_T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
TextSentencer_T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
TextSentencer_T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
TextSentencer_T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
TextSentencer_T5 | 447-655 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. |
TextSentencer_T6 | 656-664 | Sentence | denotes | Embryol. |
TextSentencer_T7 | 665-669 | Sentence | denotes | Exp. |
TextSentencer_T8 | 670-694 | Sentence | denotes | Morphol., 87, 115-128.). |
TextSentencer_T9 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
TextSentencer_T10 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
TextSentencer_T11 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
TextSentencer_T12 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
TextSentencer_T13 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
TextSentencer_T14 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
TextSentencer_T15 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
TextSentencer_T16 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
TextSentencer_T17 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
TextSentencer_T18 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
TextSentencer_T19 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
TextSentencer_T20 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
T5 | 447-694 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. Embryol. Exp. Morphol., 87, 115-128.). |
T6 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
T7 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
T8 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
T9 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
T10 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
T11 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
T12 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
T13 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
T14 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
T15 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
T16 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
T17 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
T5 | 447-655 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. |
T6 | 656-664 | Sentence | denotes | Embryol. |
T7 | 665-669 | Sentence | denotes | Exp. |
T8 | 670-694 | Sentence | denotes | Morphol., 87, 115-128.). |
T9 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
T10 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
T11 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
T12 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
T13 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
T14 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
T15 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
T16 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
T17 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
T18 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
T19 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
T20 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
GlyCosmos15-Sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-116 | Sentence | denotes | Expression of the large I antigen forming beta-1,6-N-acetylglucosaminyltransferase in various tissues of adult mice. |
T2 | 117-234 | Sentence | denotes | Large I antigen is specifically formed by a beta-1,6-N-acetylglucosaminyltransferase (IGnT), which is a Golgi enzyme. |
T3 | 235-360 | Sentence | denotes | IGnT converts a linear carbohydrate structure, the i antigen, to a branched structure, the I antigen in N-acetyllactosamines. |
T4 | 361-446 | Sentence | denotes | This conversion has been shown to be developmentally regulated in human erythrocytes. |
T5 | 447-694 | Sentence | denotes | In mouse embryonic development, it has been shown that poly-N-acetyllactosamine plays a critical role in the compaction process (Rastan,S., Thorpe,S.J., Scudder,P., Brown,S., Gooi,H.C., and Feizi,T. (1985) J. Embryol. Exp. Morphol., 87, 115-128.). |
T6 | 695-840 | Sentence | denotes | In order to understand the regulation of IGnT expression during mouse development, the IGnT transcripts were studied using in situ hybridization. |
T7 | 841-1003 | Sentence | denotes | The cDNA encoding IGnT was isolated from a murine PCC4 teratocarcinoma cDNA library by nucleic acid hybridization using probes generated from the human IGnT cDNA. |
T8 | 1004-1144 | Sentence | denotes | The IGnT cDNA was used to produce a fusion protein, which was then used as an immunogen to produce polyclonal antibodies against the enzyme. |
T9 | 1145-1229 | Sentence | denotes | Nucleotide sequence data was used to design oligonucleotide primers and cDNA probes. |
T10 | 1230-1437 | Sentence | denotes | The primers and probes, antibodies specific to the fusion protein, and previously obtained human anti-I or i sera, were used to analyze adult and embryonic mouse tissues for expression of IGnT and I antigen. |
T11 | 1438-1587 | Sentence | denotes | To detect IGnT mRNA, in situ reverse-transcription and polymerase chain reaction were performed on tissue sections using the oligonucleotide primers. |
T12 | 1588-1672 | Sentence | denotes | Amplified DNA products were detected by in situ hybridization using the cDNA probes. |
T13 | 1673-1762 | Sentence | denotes | IGnT protein was detected by immunohistochemistry using the IGnT fusion-protein antibody. |
T14 | 1763-1847 | Sentence | denotes | Expression of the carbohydrate structures was detected using human anti-I or i sera. |
T15 | 1848-1956 | Sentence | denotes | The results presented demonstrate that IGnT and the I antigen appear in epithelial cells and dividing cells. |
T16 | 1957-2049 | Sentence | denotes | The antigen also appears to be expressed on cells exposed to the lumenal surface of tissues. |
T17 | 2050-2225 | Sentence | denotes | These results support the conclusions obtained by the previous studies that IGnT and the resultant I antigen may play critical roles during development and in adult organisms. |
GlyCosmos15-GlycoEpitope
Id | Subject | Object | Predicate | Lexical cue | glycoepitope_id |
---|---|---|---|---|---|
T1 | 24-33 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T2 | 123-132 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T3 | 286-295 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | i antigen | http://www.glycoepitope.jp/epitopes/EP0139 |
T4 | 326-335 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T5 | 1427-1436 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T6 | 1900-1909 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
T7 | 2149-2158 | http://purl.jp/bio/12/glyco/glycan#Glycan_epitope | denotes | I antigen | http://www.glycoepitope.jp/epitopes/EP0138 |
GlyCosmos15-MONDO
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 896-911 | Disease | denotes | teratocarcinoma | MONDO:0002599 |
GlyCosmos15-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 221-226 | Body_part | denotes | Golgi | http://purl.obolibrary.org/obo/GO_0005794 |
T2 | 433-445 | Body_part | denotes | erythrocytes | http://purl.obolibrary.org/obo/CL_0000232 |
T3 | 1537-1543 | Body_part | denotes | tissue | http://purl.obolibrary.org/obo/UBERON_0000479 |
T4 | 1920-1936 | Body_part | denotes | epithelial cells | http://purl.obolibrary.org/obo/CL_0000066 |
T5 | 2209-2224 | Body_part | denotes | adult organisms | http://purl.obolibrary.org/obo/UBERON_0007023 |
GlyCosmos15-FMA
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 94-101 | Body_part | denotes | tissues | FMA:9637 |
T2 | 433-445 | Body_part | denotes | erythrocytes | FMA:62845 |
T3 | 1392-1399 | Body_part | denotes | tissues | FMA:9637 |
T4 | 1537-1543 | Body_part | denotes | tissue | FMA:9637 |
T5 | 1920-1936 | Body_part | denotes | epithelial cells | FMA:66768 |
T6 | 2030-2048 | Body_part | denotes | surface of tissues | FMA:67640 |
GlyCosmos15-Glycan
Id | Subject | Object | Predicate | Lexical cue | image |
---|---|---|---|---|---|
T1 | 24-33 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T2 | 123-132 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T3 | 286-295 | Glycan | denotes | i antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G00058MO |
T4 | 326-335 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T5 | 1427-1436 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T6 | 1900-1909 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
T7 | 2149-2158 | Glycan | denotes | I antigen | https://api.glycosmos.org/wurcs2image/latest/png/binary/G56045WU |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 111-115 | OrganismTaxon | denotes | mice | 10088 |
T2 | 427-432 | OrganismTaxon | denotes | human | 9606 |
T3 | 450-455 | OrganismTaxon | denotes | mouse | 10088|10090 |
T5 | 759-764 | OrganismTaxon | denotes | mouse | 10088|10090 |
T7 | 987-992 | OrganismTaxon | denotes | human | 9606 |
T8 | 1321-1326 | OrganismTaxon | denotes | human | 9606 |
T9 | 1386-1391 | OrganismTaxon | denotes | mouse | 10088|10090 |
T11 | 1824-1829 | OrganismTaxon | denotes | human | 9606 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 221-226 | Body_part | denotes | Golgi | http://purl.obolibrary.org/obo/GO_0005794 |
T2 | 433-445 | Body_part | denotes | erythrocytes | http://purl.obolibrary.org/obo/CL_0000232 |
T3 | 1537-1543 | Body_part | denotes | tissue | http://purl.obolibrary.org/obo/UBERON_0000479 |
T4 | 1920-1936 | Body_part | denotes | epithelial cells | http://purl.obolibrary.org/obo/CL_0000066 |
T5 | 2209-2224 | Body_part | denotes | adult organisms | http://purl.obolibrary.org/obo/UBERON_0007023 |
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 433-445 | Cell | denotes | erythrocytes | http://purl.obolibrary.org/obo/CL:0000232 |
T2 | 502-506 | Cell | denotes | poly | http://purl.obolibrary.org/obo/CL:0000096|http://purl.obolibrary.org/obo/CL:0000775 |
T4 | 1920-1936 | Cell | denotes | epithelial cells | http://purl.obolibrary.org/obo/CL:0000066 |